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nsv5456457

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:113

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 101 SVs from 20 studies. See in: genome view    
Submitted genomic66,174,155-66,174,267Question Mark
Overlapping variant regions from other studies: 101 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):65,469,983-65,470,095Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5456457Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr566,174,15566,174,267
nsv5456457RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr565,469,98365,470,095

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16966091duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16966091Submitted genomicNC_000005.10:g.661
74155_66174267dup
GRCh38 (hg38)NC_000005.10Chr566,174,15566,174,267
nssv16966091RemappedPerfectNC_000005.9:g.6546
9983_65470095dup
GRCh37.p13First PassNC_000005.9Chr565,469,98365,470,095

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv169660910.012796404
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